Hypertension (Dallas, Tex. : 1979) · 2015
Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing Adenoma.
Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Fernandes-Rosa Fabio Luiz, Giscos-Douriez Isabelle, Amar Laurence, Gomez-Sanchez Celso E, Meatchi Tchao, Boulkroun Sheerazed, Zennaro Maria-Christina
Аннотация
Primary aldosteronism is the most common form of secondary hypertension. Somatic mutations in KCNJ5, ATP1A1, ATP2B3, and CACNA1D are found in aldosterone-producing adenoma. In addition, adrenals with aldosterone-producing adenomas show cortical remodeling and frequently multiple secondary nodules. Our aim was to investigate whether different aldosterone-producing nodules from the same adrenal share the same mutational status. Aldosterone synthase expression was assessed in multinodular adrenals from 27 patients. DNA of 37 aldosterone-producing secondary nodules was extracted from formalin-fixed paraffin-embedded tissues and genotyped for KCNJ5, ATP1A1, ATP2B3, and CACNA1D mutations. Among 17 adrenals with a somatic mutation in the principal nodule, 4 showed the same mutation in a secondary nodule, whereas 10 had no mutation in any of the known genes. In 1 adrenal harboring the KCNJ5 p.Gly151Arg mutation in the principal nodule, the same mutation was present in 2 secondary nodules, but no mutation was found in a third nodule. Finally, in 2 adrenals with a CACNA1D mutation in the principal nodule, a KCNJ5 mutation was identified in the secondary nodule. Among 10 adrenals without mutations in the principal nodule, 1 carried a KCNJ5 mutation in the secondary nodule. No mutations were detected in 7 aldosterone-producing cell clusters from 6 adrenals. No association was observed between the presence of mutations in secondary nodules and clinical parameters. In conclusion, different mutations are found in different aldosterone-producing nodules from the same adrenal, suggesting that somatic mutations are independent events triggered by mechanisms that remain to be identified.
Предметные рубрики MeSH
Adrenal CortexAdrenal Cortex NeoplasmsAdrenal GlandsAdrenocortical AdenomaAdultAldosteroneAllelesCalcium Channels, L-TypeCohort StudiesFemaleG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGenotypeHumansHyperaldosteronismMaleMiddle AgedMutationPlasma Membrane Calcium-Transporting ATPasesRetrospective StudiesSodium-Potassium-Exchanging ATPase